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Children Coping With A Parents Terminal Illness
- 1. Downloaded from caonline.amcancersoc.org by on January 21, 2010 (©American Cancer Society, Inc.)
Current Approaches to Helping Children Cope with a Parent’s Terminal Illness
Grace H. Christ and Adolph E. Christ
CA Cancer J Clin 2006;56;197-212
DOI: 10.3322/canjclin.56.4.197
This information is current as of January 21, 2010
The online version of this article, along with updated information and services, is
located on the World Wide Web at:
http://caonline.amcancersoc.org/cgi/content/full/56/4/197
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Williams Street NW, Atlanta GA 30303. (©American Cancer Society, Inc.) All rights reserved.
Print ISSN: 0007-9235. Online ISSN: 1542-4863.
- 2. CA Cancer J Clin 2006;56:197–212
Current Approaches to Helping
Children Cope with a Parent’s
Terminal Illness1
Grace H. Christ, MSW, DSW; Adolph E. Christ, MD, DMS
Downloaded from caonline.amcancersoc.org by on January 21, 2010 (©American Cancer Society, Inc.)
Dr. G. Christ is Associate Profes-
ABSTRACT Much has been learned about childhood bereavement in the last few decades as sor, Columbia University School of
studies have increasingly focused on the direct interviewing of children about their recovery from Social Work, New York, NY.
the tragic loss of a parent. It has been shown that children do indeed mourn, although differently Dr. A. Christ is Professor Emeritus,
Child/Adolescent Psychiatry SUNY
from adults. Important moderating and mediating variables have been identified that impact Health Science Center at Brooklyn
their recovery from the loss of a parent, which can be the focus of intervention. When death is and Kings County Hospital, Brook-
lyn, NY.
expected, the terminal phase of an illness has been found to be particularly stressful for children,
This article is available online at
yet seldom investigated. Similarly, few studies have explored the impact of development on http://CAonline.AmCancerSoc.org
children’s experience and expression of grief. We present research findings that clarify phases
in children’s experience during the terminal illness, hospital visits, the death, and its immediate
aftermath, as well as how the parent is mourned and issues in longer term reconstitution. Variations in children’s responses in these
phases are described as they were experienced by 87 children from 3 different developmental groupings: 3 to 5 years, 6 to 8 years,
and 9 to 11 years. Recommendations are suggested for parents and professionals about ways to understand and support children
during the terminal illness, at the time of death, and during the phase of reconstitution. (CA Cancer J Clin 2006;56:197–212.)
© American Cancer Society, Inc., 2006.
INTRODUCTION
For a child, the death of a parent is a highly stressful event. Research suggests that it places them at risk for adverse
psychosocial consequences. However, with adequate family resources, competent substitute care, and emotional
support, bereaved children are better able to return to previous levels of functioning.1– 4 When death can be
anticipated, as with a terminal illness, physicians and other health care professionals have an opportunity to ameliorate
the impact of the loss. The experiences of adolescents who confront parent loss from illness and the ways professionals
can support their coping were reviewed in an earlier article.5 Presented here is an update on current approaches to
helping children (age 3 to 5, 6 to 8, and 9 to 11) cope with a parent’s terminal cancer illness and death. These
approaches are informed by three areas of research:
Y Risk and protective factors that mediate the coping of bereaved children.
Y Intervention during the terminal illness.
Y Developmental grouping of children to enhance specificity and accuracy of findings and interventions.
Suggested are ways to better prepare families and health care professionals to facilitate children’s mastery of
adaptive tasks during the terminal phase of the parent’s illness, at the death, and during its immediate aftermath.
1
This work was supported in part by grants from the National Institute of Mental Health (NIMH) (MH41967), the American Cancer Society (PRB-24A), the
van Ameringen Foundation, the Society of Memorial Sloan-Kettering Cancer Center, and the Project on Death in America of the Open Society Institute.
Volume 56 Y Number 4 Y July/August 2006 197
- 3. Helping Children Cope with a Parent’s Terminal Illness
BACKGROUND Recent studies have also identified a broad
range of risk and protective factors that con-
Early research in childhood bereavement tinue to be explored, refined, and utilized in
hypothesized links between unresolved child- developing interventions and service programs.
hood grief and subsequent adult psychopathol- Those currently under study are summarized in
ogy.6 – 8 While early studies appeared to Table 1. Prospective and retrospective studies
establish a link,9,10 later research was able to confirm the critical role of the surviving parent
control for independent, moderating, and me- or caregiver in helping children adapt to a
diating variables associated with outcomes that
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parent’s death. The quality of the relationship
suggested child bereavement alone was un- with the surviving parent or caregiver and their
likely to be related to adult psychopathology.11 competence in parenting bereaved children are
Rather, these studies highlighted the impor- the most consistently identified mediating vari-
tance of mediating and moderating factors as- ables.3,15–20 Caregiver attributes that contrib-
sociated with bereavement, such as the quality ute to children’s adaptation include more active
of parental care and the presence of other ad- coping, less depression, more parental warmth,
verse social and psychological occurrences pre- and family cohesiveness.4,20 While the connec-
ceding and following the bereavement that tion between children’s mourning experience
may have more influence on adult outcomes and adaptation level has not been clearly doc-
than the fact of the death.12 umented, better psychological outcomes have
Studies conducted shortly after parent death, been associated with broader characteristics, in-
including interviews with children, have con- cluding openness of general communication
firmed that children do indeed experience with the surviving parent and sharing of infor-
grief, sadness, and despair following the death mation about the parent’s death.21,22 Parents
of a parent. As Dowdney states in her review of often find it difficult to understand and respond
child bereavement research, “Inconsistencies in to their children’s unique, developmentally
the literature relate to rates of disorder or dis- specific expressions of grief, which may seem
turbance rather than to the manner in which vague, intermittent, and at times inappropriate
children manifest distress.”8 The highest rates by adult standards. Adults find that children can
of psychological symptoms are found in sam- even appear to be unconcerned, callous, or
ples that include children referred for bereave- indifferent.
ment services or those from less stable
backgrounds or under-resourced family envi- Helping Children Cope During the Parent’s
ronments.8,13,14 In adequately resourced and Terminal Illness
stable family situations, those with clinical level
symptoms extending beyond 1 year after the The surviving parent’s management of the
death of a parent are about 20%. For example, terminal illness experience and preparation of
Lin reported that 40% of bereaved children had their children for the death are viewed in the
clinical symptom levels in a sample of children clinical literature as important mediators of
whose families were seeking bereavement ser- children’s bereavement, yet there has been little
vices and who were subsequently entered into investigation of the children’s coping during
a parent-child skills training program.4 By con- this time period. Siegel reports that children
trast, the Harvard Bereavement Study reported (age 7 to 17) whose parents were in the termi-
only 19% of their publicly recruited sample of nal stages of illness displayed significantly
bereaved children had clinical symptom levels higher levels of depression and anxiety than
on the same measure at approximately the same community controls.23 At follow up, between
time since the parent’s death.13 These studies 7 and 12 months after parental death, differ-
do not include longer-term outcomes. One ences between the groups had become nonsig-
study reported an elevation of symptoms 2 nificant.3 These findings suggest that when
years after the parent’s death, suggesting the parental death follows a lengthy terminal ill-
possibility of later consequences.13 ness, child disturbance may precede the death
198 CA A Cancer Journal for Clinicians
- 4. CA Cancer J Clin 2006;56:197–212
TABLE 1 Risk Factors Impeding and Protective Factors Promoting Reconstitution
Risk Factors Impeding Reconstitution
Concurrent stressful life events
A negative or non-supportive relationship with the surviving caregiver
A poor relationship with the parent who died
Low self-esteem and an external locus of control
Preexisting mental health problems in the adolescent or the surviving parent or caregiver
Circumstances of the death, such as violent or traumatic death
Protective Factors Promoting Reconstitution
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Having a relationship with surviving parent or caregiver characterized by open communication, warmth, and positive experiences
Surviving parent able to sustain parenting competence
Feeling accepted by peers and other adults, such as relatives and teachers
Higher socioeconomic status
Internal locus of control, religiousness
Intellectual and social competence
The opportunity to express thoughts and feelings about the deceased parent and have them validated by others
itself. Indeed, for children it may be the time of encouraging adaptive denial to permit quality
highest distress. Other recent retrospective time together while symptoms are reduced.
studies of bereaved children continue to doc- Many parents strive to limit the adverse im-
ument misunderstandings and guilt surround- pact of the loss on their children’s future de-
ing the parent’s deteriorating condition and velopment and frequently request guidance
terminal illness.24,25 These studies also reported from physicians about how best to communi-
bereaved children’s memories of anxiety and cate with their children during the parent’s
disappointment when visiting and interacting terminal illness.3,24,28,29 Children and adoles-
with the ill parent, memories that remained cents report that they value open communica-
painful and disturbing during the first years tion with both parents about the illness and
after the death. death, and research suggests that it helps them
Few interventions have been developed to during their bereavement.21,26 Younger chil-
address these stresses and parenting challenges. dren are less likely than adolescents to receive
Only one intervention studied focused on information about their parent’s terminal con-
helping surviving parents achieve effective dition before the death.22 This is thought to
communication with their children about the occur because young children have less access
patient’s impending death, including mediating to adult information, their more limited cog-
successful visits when the patient was in the nitive abilities make it difficult to explain the
hospital.26 Newer medical treatments have ex- situation to them, and adults, often incorrectly,
tended the terminal illness period for many believe they are protecting them from the
cancer patients so that it may now include emotional pain of loss by not discussing it with
periods of disease exacerbation and aggressive them ahead of time. As a consequence, chil-
treatment, alternating with periods of reduced dren’s particular questions and needs during
symptoms and disease control when life can their parent’s terminal illness are less under-
proceed more normally. This gives families stood.
much needed hope, but also creates new adap-
tive challenges. Determining prognosis, that is, Age-specific Information
when death is imminent is increasingly diffi-
cult.27 Both parents and physicians must find When death is imminent, physicians and
new ways to communicate about the illness, other health professionals can help prepare par-
explaining what children see and hear and pre- ents by providing specific, concrete informa-
paring them for difficult times, but also reas- tion and practical advice to facilitate coping and
suring them of the parent’s well-being when meeting children’s needs at this very stressful
their condition is stable or has improved and time in the family’s life. Unfortunately, re-
Volume 56 Y Number 4 Y July/August 2006 199
- 5. Helping Children Cope with a Parent’s Terminal Illness
search on developmentally specific responses, portive intervention) conducted with families
although requested by parents, has been lim- beginning 3 to 6 months before the patient
ited. While clinical case studies have reported died and continuing for 14 months after death
different cognitive and emotional responses of from cancer.26 Families with children who had
preschoolers, school-age children, and adoles- a serious preexisting emotional problem were
cents, no differences in disturbance by age have excluded. This more homogeneous population
been established.8,30 A study of bereaved 3- to made it possible to group children with similar
5-year-old children found that, contrary to the cognitive, emotional, and sociocultural devel-
opmental attributes.1 As presented below, this
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guilt generally described in older children’s
grief, children this age experienced no feelings grouping clarified clinically important differ-
of causal responsibility.31 Rather they are re- ences in their responses to the illness and death
ported to show separation anxiety, depen- of a parent. The exclusion of unpredictable
dency, nighttime fears, regressive behaviors, deaths also made it possible to understand the
irritability, and impatience.32,33 Another age- impact of the highly stressful reactions to the
specific study focused on bereaved adolescents. terminal illness and the value of providing in-
Adolescents younger than 15 years old at the terventions during this critical stage.
time of the parent’s death were found to be A qualitative analysis was used with the in-
more vulnerable to depression than those 15 to tervention interviews of 157 children from 88
19 years of age.34,35 Other clinical literature has families. Five different developmental group-
attempted to clarify the grief process during ings were identified: 3 to 5 years, 6 to 8 years,
adolescence, but the specific effects of parental 9 to 11 years, 12 to 14 years, and 15 to 17
death on the mental health of this age group years.1,26 The categories were formed by
have remained largely unexplored. grouping children who evidenced similar de-
velopmental attributes. The parent-guidance
intervention focused on family communication
NEW DIRECTIONS
about the illness, parental competence with
Three National Institute of Mental Health their bereaved children, and promoting consis-
(NIMH)-supported studies addressed child be- tency in management of family decision mak-
reavement issues using prospective rather than ing and direction.36 Information was also
retrospective designs.2,13,36 Two programs obtained from parent and child assessments be-
studied families following the death of a parent fore and after the parent’s death. The findings
to provide generalizable information about the describe children’s experiences and related in-
response and recovery processes of expected terventions at three different time periods: (1)
and unexpected deaths, including those from when the patient was believed to have a life
accident, suicide, and homicide. Worden’s expectancy of at least 6 months;38 (2) at the
Harvard Child Bereavement Study yielded im- time of the patient’s death; and (3) during the
portant insights about the recovery processes immediate bereavement period.
reviewed above. Children and adolescents
were more symptomatic at the second than
DEVELOPMENTAL VARIATIONS IN CHILDREN’S
after the first anniversary of the parent’s RESPONSES TO A PARENT’S TERMINAL ILLNESS
death.13,37 Sandler provided a carefully con-
trolled parent and child skills training interven- Sample
tion. Families were recruited from those
seeking preventive bereavement services, and The sample in the MSKCC study included
these distressed families improved following a both children and adolescents. The findings
series of 12 group sessions.2 presented here were drawn from the 87 3- to
The Memorial Sloan-Kettering Cancer 11-year-old children whose families partici-
Center study (MSKCC) compared 2 interven- pated in the parent-guidance intervention.
tions (a parent-guidance and a telephone sup- There were 11 girls and 7 boys in the 3- to
200 CA A Cancer Journal for Clinicians
- 6. CA Cancer J Clin 2006;56:197–212
5-year-old group; 16 girls and 16 boys in the 6- ited understanding. Nevertheless, it is often
to 8-year-old group, and 18 girls and 19 boys in helpful for parents to give children a script, an
the 9- to 11-year-old group. explanation of events that they more fully grasp
as they mature.
A 7-year-old said of her 4-year-old sister,
THREE- TO FIVE-YEAR-OLD CHILDREN: “WHERE DID “Before my mother died, my sister wanted to
HE GO?”
talk about her death, because she thought it was
Key Developmental Characteristics like an exciting thing. She thought she would
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come back. Now she’s mad because she didn’t
Y Early preoperational thinking39 makes it dif- come back.”
ficult for them to understand the meaning of Another 7-year-old described her 4-year-
the illness and the permanence of death. old sister’s reaction: “The night Daddy died,
Y They can repeat a memorized script that she and Mummy came to my bed. Mummy
explains the situation, but without under- said, ‘Your father died,’ and my sister was
standing it. laughing because she thought something excit-
Y Communication is mostly through play and ing had happened. She didn’t know what dead
fantasy. means. It was very sad; Mummy cried until the
Y Limited language skills make it hard for priest came, then my sister cried too.” The
caregivers to comprehend young children’s mother added, “She cried because I cried.”
behaviors and moods. During a father’s terminal illness, one
Y Their world consists almost exclusively of 4-year-old expressed her anxiety about his ob-
family centered around the home and their vious frailty by describing her new imaginary
relationship to the primary caregiver(s). companions, brothers and sisters who became
Y Separation from a primary caregiver is their ill and died and were immediately replaced
greatest source of stress. Even very young with new “bigger and stronger brothers” who
children can experience night terrors and watched over her and took care of her. This
other more obvious distress responses related play lasted several weeks and was gradually
to the sudden and frequent removal of a elaborated as her father’s illness progressed. It
primary caregiver. seemed to reflect her anxiety about his symp-
Y Fortunately, children this age can accept toms, the well parent’s distress, and her belief
competent substitute caregivers, especially if and wish that the father would return and be
prepared for the possibility of unexpected able to take care of her again.
substitutions. It is important with children this age to
Y Young children can become distressed by locate a competent substitute caregiver when
the primary caregiver’s outbursts of grief, necessary and repetitively reassure children that
their inability to mute or filter strong reac- they are loved and will be taken care of.
tions, or their emotional withdrawal from
illness or exhaustion. Planning Hospital Visits
Intervention during the Parent’s Terminal Illness Some parents misunderstand “open com-
munication” to mean the full expression of
Three- to five-year-old children can observe their intense grief with young children. One
the parent’s loss of strength and function, such 3-year-old developed a fear of entering her
as the inability to lift them. “Daddy can’t take father’s hospital room because her young par-
care of me anymore,” said a 3-year-old who ents tended to cry together when she was there.
observed her father’s difficulty with ambula- The mother was referred to a social worker
tion. They begin to understand that something who helped her structure the visits, control her
is wrong, but cannot comprehend the perma- strong emotions, limit the time of the visits,
nence of death. If the parent discusses it with and bring things for the daughter to do with
them, they might say the words, but with lim- her father. The child’s fears decreased and the
Volume 56 Y Number 4 Y July/August 2006 201
- 7. Helping Children Cope with a Parent’s Terminal Illness
visits were often pleasurable. If the parent is in things in the coffin with the parent (eg, stuffed
the hospital for an extended period of time, animals, pillows, pictures of the parent, or toys
young children can be relieved to see them, the child especially likes).
however briefly. As children this age experience the parent
At times, parents resist having their young not returning day after day, they may become
child see them in a debilitated state. If the increasingly angry and distraught over time.
parent, child, and hospital staff were prepared, Older siblings can become impatient with hav-
the visit structured, and the patient’s condition ing to answer their demanding questions.
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explained by staff, the visit was positive, and One 4-year-old girl became whiny and
the patient was not remembered in a negative clingy after her father died. Occasionally, she
way.1 Children generally develop positive sat in his chair with many blankets wrapped
memories and images of the parent shortly after around her. When she began complaining of
the death. At times a parent resists contact stomach aches, her mother took her to the
when in a debilitated state because they do not doctor, and she promptly asked him when she
want to risk infection by handling a child or could see her father again. Three months later,
they have no energy to cope with a child’s she was able to say, “Daddy died.”
emotion and developmentally appropriate
physical demands. These situations must be ex- How the Parent is Remembered
plained to children to counter their feeling that
they are being rejected because they are bad. The children’s memories of the deceased
The patient’s vulnerability must also be re- parent were generally positive soon after the
spected. Alternative modes of communication death, focusing on pleasurable experiences,
(eg, telephone, note cards, or gifts) can be caretaking, and protective functions. Many
helpful. loved to hear stories about the deceased parent.
One 4-year-old enjoyed when her sister made
The Death and Its Immediate Aftermath their father’s favorite pancakes using his “se-
cret” recipe or when they carefully tended
When death occurs, children in this age Daddy’s garden. Another 4-year-old recalled
range require concrete descriptions of what that his father had tickled him; another talked
happens to people when they die—loss of with pleasure about how his father had tossed
functions, permanence of the death, as well as him up in the air. Recapturing such experi-
sadness and other emotions people feel after the ences seemed to comfort them. However, after
death. When told of the parent’s death, chil- some time, most children this age requested
dren this age are often befuddled, wondering that the surviving parent find a replacement.
where the parent has gone. Repetitive ques- Young children wanted a whole family, like
tioning about where the parent has gone is the other children in their preschools had.
characteristic for weeks and months after the One 5-year-old said, “Next time, get two
death. Although such questioning helps chil- daddies, so if you lose one again.”
dren this age develop a sense of mastery, it can
evoke overwhelming emotions in the grieving, The Course of Recovery: Issues in Reconstitution
surviving parent. Having children participate in
bereavement play groups or talk with another One mother explained that her 4-year-old
adult about the parent who died, like aunts or son was not mourning. Rather, he seemed very
uncles of the deceased parent, especially telling happy because she was now home much more
stories about the parent, can provide opportu- regularly than she had been during his father’s
nities to support the child and at the same time terminal illness. The central focus of children
relieve the grieving parent. Children this age this age on the primary caregiver meant that
often enjoy bereavement groups, relevant art their consistent and predictable presence was
therapy, or other expressive sessions after death essential. The primary caregiver often needed
has occurred. Many children also want to place to function as a “Rosetta Stone,” helping to
202 CA A Cancer Journal for Clinicians
- 8. CA Cancer J Clin 2006;56:197–212
interpret the child’s behaviors and affects to elaborate eavesdropping methods, picking up
others, as well as to the child. extension phones, and listening through closet
walls. However, we observed that if parents
spoke candidly and explained major changes
SIX- TO EIGHT-YEAR-OLD CHILDREN: “I THINK I directly, children then felt free to ask questions,
KILLED HER”
and misunderstandings could be clarified.
Key Developmental Characteristics
In this age range, children’s awareness of
their parent’s death can be quite varied. Many
spoke openly about being afraid their parent
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Y Late preoperational thinking39 includes both
magical and logical thinking. would die, even when their parents had previ-
Y Children understand the parent will not re- ously told clinicians they thought their children
turn and death is universal (it could happen “had no idea” about the parent’s diagnosis and
to me). did not understand about their imminent
Y Children may be highly emotional and have death. Other children, though aware of the
difficulty containing emotions. illness, were unaware of the terminal nature of
Y They blame themselves when bad things the current episode. A few were unclear about
happen. the diagnosis and therefore were confused
Y They may make logical errors, misunder- about what was happening to the parent. Most
standing cause and effect. had “anticipatory anxiety” rather than antici-
Y They can show fear that aggressive thoughts, patory grief as experienced by adolescents and
words, or wishes can be harmful. adults. They sensed something “catastrophic”
Y “I prayed my mother would be out of pain was going to happen, and they wondered if
the night before she died. I think I killed they or their family would survive it.
her,” said a 7-year-old girl. An 8-year-old boy whose father was termi-
Y They cannot retrace thinking to origins of nally ill said, “I began to think maybe Grandma
error to correct erroneous ideas. and Grandpa would die, my mom would also
Y Parental support of self-esteem is still die, and maybe the whole world would end,
needed, but now they are also aided by and nothing would be there.”
praise of teachers. These children tend to be highly emotional
Y Although parents are a primary source of and reactive to the many changes taking place
self-esteem, they fear rejection by peers. in the family as a consequence of the parent’s
Y A 7-year-old girl cried because a classmate illness. Indeed, this seems the most difficult age
said, “You can’t go to the father-daughter for parents to manage during the predeath pe-
dance because your daddy is dead!” riod, even though existing research has not
Y Language skills are more advanced. necessarily identified them to be at higher risk
over the long term. They are upset by both
Intervention during the Parent’s Terminal Illness parents’ preoccupation with the ill patient’s
condition and their difficulty in listening to the
Three types of information are helpful to 6- child or playing with them. They react to sep-
to 8-year-old children during the parent’s ter- arations and to changes in their own activities.
minal illness: (1) simple, concrete, definitional, They react to the parents’ increased tension,
disease-related information, such as the name anger, and depression, and to the lack of hap-
of the disease, its progress, symptoms, treat- piness, joy, and celebrations in the home. Ex-
ments and causes; (2) simple explanation of the planation of what is happening, even if the
causal relationship between the patient’s be- child does not ask, is often helpful and can give
havior and appearance and the symptoms and permission for the child to ask more questions.
treatment of the disease; and (3) when death is Children this age find it difficult to “reverse”
imminent, the prognosis. These children may their thinking once they develop an erroneous
well overhear conversations that include this idea. Therefore, even when parents explain the
information. One 8-year-old boy developed patient’s withdrawal is not from a lack of love
Volume 56 Y Number 4 Y July/August 2006 203
- 9. Helping Children Cope with a Parent’s Terminal Illness
and that the illness causes these changes, they the clinician asked how they were feeling about
may remain angry and upset for some time and their mother being in the hospital, they re-
require much repetition. These children are sponded angrily that she had been there for 62
also “truth tellers” or “whistle blowers” and days. They knew that because they had been
will readily express emotions and situations crossing off the days on a calendar they brought
their older siblings have learned to hide or with them. Their behavior improved markedly
disguise. after the brief visit with their mother.
One 7-year-old girl whose father was termi- As with younger children, preparation for
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nally ill with a brain tumor described the the visit is essential. When the patient’s condi-
changes in their family. “Mom and Dad used to tion and physical state, intravenous bottle, etc.,
go dancing. They don’t do that any more, and can be explained, the interaction with children
Mom is angry all the time. Dad won’t let me sit is facilitated. Discussion afterward is easier and
on his lap. I don’t think he loves me anymore.” can more readily clarify any misunderstanding.
Parents often find it useful to enlist the help If parents cannot cope with visits, they can help
of other adults or professionals to listen to their children by telephone communication and ex-
children’s distress. The parent’s own emotional change of letters, drawings, and gifts. However,
state as the patient’s death approaches or in the seeing and hearing the patient and his or her
postdeath period may limit their capacity to caregivers in the hospital not only provide the
attend in a helpful way. child with an important confrontation with
reality, but also with reassurance that is difficult
Planning Hospital Visits to achieve in other ways.
Although the 6- to 8-year-olds do not need Saying Good-bye
the parent’s constant presence, as do 3- to
5-year-olds, they do need the parent to be as It was unusual for patients to talk with their
consistent as possible with them. For example, children this age about their own imminent
this includes letting them know about the pos- death. When an ill parent did so, the child
sibility of emergency trips to the hospital and often reminisced with pleasure about having
preparing them for how the situation will be said final good-byes to the patient. However, as
handled and who will take care of them when others have suggested, saying the word good-
both parents are absent. If separations are not bye seemed not as important as a final hug,
prolonged, and they are aware of the parents’ squeeze of the arm, and repeated affirmation of
whereabouts, they can be tolerant of temporary love.
caregivers and babysitters. However, if separa- A 6-year-old said, “I wanted to hear those
tions are prolonged, they become distressed, magic words, ‘I love you.’”
especially if they are not permitted to visit the An 8-year-old remembered his father say-
parent in the hospital. In these situations, a ing, “I love you,” to him.
planned visit can reduce their anxiety dramat- One 7-year-old remembered how she had
ically and lead to improved behavior at home. hugged her mother.
Some patients want to protect their children Another 7-year-old was comforted by re-
from their altered appearance. However, we membering that, even though her mother
found that most children this age spoke only could not talk any more, she had squeezed her
briefly after the death about the sick parent’s hand. For months, she put herself to sleep with
appearance. They were more likely to feel re- this tactile memory.
jected by the parent’s not wanting to have If children did not say good-bye to the pa-
them visit. tient directly, they were often comforted by
Six- and four-year-old brothers were re- writing their thoughts down and placing them
ported to be fighting more than usual even in the coffin. The mother of one 8-year-old
though they had a housekeeper during the day boy placed his letter in her husband’s hand in
while their mother was in the hospital. When the casket.
204 CA A Cancer Journal for Clinicians
- 10. CA Cancer J Clin 2006;56:197–212
The Death and Its Immediate Aftermath and strong, much admired hero or heroine.
Active, open, and vocal construction of this
In contrast to their younger peers, children image seems to comfort them even though
this age generally understand the finality of the such openness continues to be difficult for their
parent’s death after an illness and are appropri- grieving parent. Like their younger peers, they
ately sad and upset when informed. Many par- also request a replacement parent, less ambiv-
ents say telling their young children about the alently if the parent who died was the same
parent’s death was the most difficult task they gender as the child. They love talking about
had ever faced. These children express sadness,
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and recalling pleasant episodes they had with
anger, and dejection connected with thoughts the parent who died, surrounding themselves
about the parent, but then often quickly return with their pictures, and incorporating the par-
to normative activities. Even when they were
ent’s clothing or other objects into their play.
well prepared, some expressed surprise and
After a long parent illness, children this age
acute distress. They have more physical symp-
did express some relief that the parent had died
toms than older children, as well as fearfulness,
and was no longer suffering. They also felt
sleeping problems, and separation anxiety.
relief that they had survived what they feared
Children this age more than any other might
would be a catastrophic event.
speak openly and explicitly about wanting to
One 8-year-old said, “I can talk more about
die so they can be with or visit the parent soon
my mom now than I could before she died
after the death. Generally, these are transient
because the worst has happened and it’s over. I
thoughts and not accompanied by suicidal in-
don’t have to worry that I might make some-
tent or plans. If they persist or became rigid and
inflexible, a professional evaluation is recom- thing bad happen [by talking about it].”
mended. Their mourning is also frequently ex- Course of Recovery: Issues in Reconstitution
pressed by joyous memories of the deceased
parent, which is disconcerting to surviving As occurred in every age grouping, most of
spouses unless they understand that this is an the children returned to their previous levels of
adaptive way to retain a connection to the functioning in psychological state, relationships
parent who died. The children spoke openly with parent and siblings, academic performance
about talking with the parent who died, and for and activities, and relationships with teachers
most, these were comforting experiences. and peers by the end of the first year. It is
A 7-year-old girl told her father, “I’m going important to note that most of these families
to pray for Mommy tonight when I give the had adequate financial resources to afford hir-
blessing. Are you going to be sad?” When he
ing substitute parenting and, unlike poor or
said he would be, she brought a large box of
recent immigrant families, had few other family
tissues to the table and told him, “You always
stresses.
feel better after you cry.”
Grief with these children is usually sporadic
How the Parent is Mourned
and brief. Immersion in school and playing
with friends are common even immediately
Whatever their religion, children this age after the death and should be encouraged.
tend to locate the parent who died in a place Schools can be very helpful if teachers are no-
(usually heaven) and often with a function. tified. Many children were given permission
Most thought the parent watched over them. for short visits to school counselors when they
After receiving coins for her lost tooth, one felt sad.
7-year-old girl said, “I know where Mom is— A 7-year-old was overjoyed when one of
she’s the tooth fairy!” Her father affirmed that her friends came to the funeral and went to play
he thought her mother would love that job. with her.
The image retained of the parent is that of Another 6-year-old felt reassured and ac-
the loving caregiver, provider of good things, cepted when classmates gave her a large bowl
Volume 56 Y Number 4 Y July/August 2006 205
- 11. Helping Children Cope with a Parent’s Terminal Illness
of notes and drawings they made for her after help with the care of the ill parent; however,
her father died. they should not be left independently in
At home, bedtime is especially hard. Parents charge of a seriously ill parent.
were encouraged to spend time each night
reading a story and talking about pleasant Intervention during the Parent’s Terminal Illness
memories of the parent. Some slept with the
parent for weeks or months. Many children this age showed a need for
These children reacted more to additional carefully sequenced information about the par-
ent’s illness, treatment, and impending death.
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stress or pressure, some with increasing diffi-
culty in separating from their parent when they They were able to integrate relatively concrete
and detailed information about the illness with-
were going to school, and even more so on
out becoming overwhelmed and confused.
Mondays after a weekend at home. Parents
However, they became frustrated and angry if
sometimes included a love note with lunches
they were not given enough information. They
or gave permission for the child to call home
were unable to comprehend the context in the
for a quick chat. Limit setting, temper out-
absence of more comprehensive detail.
bursts, temporary regression like bed wetting,
An 11-year-old boy said, “Last year, Dad
and clinging were common. Parents appreci-
went to the hospital, but they didn’t tell me it
ated advice about handling those behaviors,
was cancer. I thought it was not cancer, just a
understanding them as normal, and gradually
tumor. My mom finally put it straight to me,
improving behaviors. Difficulty in concentrat-
but I had to go up to her and ask. Now that I
ing in school and a drop in grades were com-
know what’s going on, I understand. Dad used
mon, and children needed to be reassured that
to be grouchy, and I didn’t understand. I
those problems were understandable and tem-
thought he was mad about something. Now it
porary. For most children, misbehavior took
doesn’t seem that he is mad at me.”
place at home, not in school. Parents grudg-
In contrast to younger children, who could
ingly appreciated that as a better alternative. become fixated on particular erroneous ideas,
children this age were able to reverse their
NINE- TO ELEVEN-YEAR-OLD CHILDREN: THE
thinking and correct logical errors.
YOUNG SCIENTIST A 9-year-old girl described how she was
different from her 6-year-old sister. “She is
Key Developmental Features much younger, and she doesn’t take things as
well as me, she doesn’t understand.” She ex-
Y There is a major change in thinking ability plained that when her parents clarified the fact
(concrete operational)—these children can that she was not responsible for her mother’s
use logical thinking, understand cause and illness, she believed them, but her sister was not
effect, and retrace memories to reverse and so sure. “I know it’s not my fault, and I
correct erroneous conclusions. couldn’t have done nothing to prevent it. It
Y Unlike early adolescents, they cannot draw wasn’t our fault.”
inferences from insufficient information. The importance of incremental information
They need detailed, concrete explanations was highlighted by a study of the responses of
about the parent’s illness and course of treat- children this age who lost parents in or had
ment to understand and feel a sense of con- high exposure to the 9/11 World Trade Center
trol. attacks. The bereaved children this age were
Y In contrast to younger children, they are the most symptomatic group of children in
able to use compartmentalization and dis- citywide school surveys.40 The total unexpect-
traction to avoid strong emotion. edness of the event deprived them of their
Y They may have outbursts of emotion fol- ability to learn incrementally, and they were
lowed by embarrassment and avoidance. overwhelmed with the complexity of the event
Y These children benefit from being able to and the enormity of the loss. In contrast, the
206 CA A Cancer Journal for Clinicians
- 12. CA Cancer J Clin 2006;56:197–212
children this age whose parents died of cancer pearance and ability to function, the reduction
and who received continuous small doses of in family activities and trips, and the prospect of
information about the progression of the illness a future without the parent’s assistance, sup-
were among the best adjusted of the five de- port, and love. They experienced some sepa-
velopmentally derived subgroups. ration anxiety when the patient was in the
Some children in this age group expressed hospital a long time and the well parent spent a
sadness about the parent’s expected death great deal of time there as well. Hospital visits
rather than only the anxiety experienced by seemed helpful, especially when they included
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younger children. They were the first group to contact with medical and nursing staff who
consistently anticipate the death and feel sad could explain the care and treatment their par-
about the future loss. ent was receiving. They even seemed to benefit
After a mother told her 10-year-old boy that from walking around the hospital and becom-
his father’s current treatment was ineffective, ing familiar with the patient’s environment.
he wanted to look at photographs of his father Learning details and facts about the place, the
as he had been before the illness. He said he treatment, and the care helped them compre-
thought about his father a lot and worried hend the context and achieve some sense of
about him. He also wondered, “Who will play relief and control. However, as with younger
basketball with me? Who will fix my bike?” He children, preparing the patient, parent, and staff
thought he would want to be with his father for the visit helped to avoid misunderstandings.
when he died. Careful preparation by the clinicians in the
Many children had difficulty in school during MSKCC study may have prevented the nega-
the terminal illness, but some children in this age tive results of hospital visits that have been
group were able to improve their performance, reported in retrospective studies.24,25 For ex-
sometimes as a gift to the ill parent. It was also not ample, some children were struggling with a
unusual for these children to offer to help out drop in grades when their parent was hospital-
with taking care of the sick parent. ized, and they feared their sick parent was
A 10-year-old boy volunteered to sleep in disappointed in their performance. The parent
the den with his father, waking up every 3 or 4 needed to understand that it was normal to
hours to give him medication. He said he liked have declines in grades at this time, an expected
to help. consequence of the love and worry of their
An 11-year-old girl became so expert at help- child, and that it was important to praise their
ing to transverse her father from the bed to a efforts during the difficulties of parent illness.
wheelchair or stretcher that she instructed the Children also valued the exchange of gifts and
ambulance workers how to best do it when they cards. Children this age seemed to find final
came to take him to the hospital. Her father was visits meaningful even when little communica-
very proud of her special competence. tion was possible. They provided concrete ev-
However, parents are cautioned about the idence of the reality that the patient was dying
importance of not leaving a child of this age and gave them an opportunity for final inter-
placed independently in charge of the care of a action.
terminally ill parent. Unfortunately, where fi-
nancial resources are inadequate, this does oc- The Death and Its Immediate Aftermath
cur. It places a heavy burden on the child with
commonly symptomatic outcomes and com- It was viewed as optimal when a child said
plicated bereavement if prolonged or when on hearing of the parent’s death, “I was sur-
mistakes are made and the parent then dies. prised, but I knew it [the death] was going to
happen because my mother kept me in-
Planning Hospital Visits formed.” Still, managing intense emotions for
children this age was difficult. Some had un-
Children this age were more distressed than usually strong reactions, which they later dis-
younger children by the parent’s changing ap- avowed.
Volume 56 Y Number 4 Y July/August 2006 207
- 13. Helping Children Cope with a Parent’s Terminal Illness
One 11-year-old boy locked himself in his who died as watching them when they were
room when his mother came home from the succeeding at school or in sports and imagined
hospital because he didn’t want to hear the the parent being pleased with their perfor-
news until he was ready. Later, he was embar- mance. Rather than focusing only on the par-
rassed about this behavior. ent’s caretaking role, as did their younger peers,
Wanting to be alone for a while was not they retained an image of the parent as teacher,
unusual. Some children cried or screamed. One coach, advocate, and friend. The mother was
boy laughed—an expression of acute anxiety. often remembered as the family organizer, love
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They needed time to collect themselves. giver, cheerleader, protector, and someone
An 11-year-old girl was at school when her with whom they could chat. Requesting a re-
mother came to tell her that her father had died placement parent was quite uncommon in
after 2 years of struggle with a brain tumor. She comparison to younger children. If it occurred,
asked to be able to remain in school with her it seemed related to more practical needs, such
friends and to complete a test in her last class. as relieving chores, helping with homework, or
She thought her father would have been proud sports.
of her good grades during such a difficult time. Like their younger siblings, these youngsters
Children this age often avoided their own also like to hear stories about the deceased
and others’ strong emotions, especially those parent. The more realistic appraisal of 9- to
related to grief. Participation in bereavement 11-year-olds is highlighted by humor, as in the
groups or programs could help them to be- following episode:
come more open, but often their feelings were An 11-year-old boy, his mother, and older
expressed in more indirect ways, as by being siblings were watching the meteor shower
messy, stubborn, argumentative, or more with- shortly after the father’s funeral. The 11-year-
drawn. They tended to control their grief by old had put two small bottles of his father’s
compartmentalizing— escaping by immersion favorite whisky in his casket. Now he pointed
in school and extracurricular activities. Diffi- out one star that seemed to careen out of
culties with sleeping were ubiquitous; some control; “That’s Dad up there— he found my
also developed phobias and fears or a preoccu- bottles of whisky.”
pation with ghosts.
These children treasured clothing and other Course of Recovery: Issues in Reconstitution
items that had belonged to the parent. They
provided comfort and opportunities to remi- The course of recovery of 9- to 11-year-old
nisce about the parent, especially during the children has much in common with that of
first year. They enjoyed looking at pictures of their younger and older peers. Unique to this
their parent in healthier and happier days, but age group are emphases on new developmental
often in more private and less expressive ways capacities: educational, recreational, and social
than did younger children. competencies. The stresses of the terminal ill-
ness and the death result for many children in
How the Parent is Mourned temporary depression, anhedonia, preoccupa-
tion, and reduction in ability to concentrate.
Like their younger peers, many children this This sequence of responses can affect all do-
age left notes and gifts in the coffin with their mains (educational, recreational, social, and
dead parent that reflected activities they en- emotional). An important process of reconsti-
gaged in together—a baseball, a letter. Many tution is the gradual regaining of competence
listened intently to eulogies and remembered in these areas of great importance to children.
them. Some children this age organized their The initial explosive outbursts, withdrawal,
own memorial services with their peers, giving and anhedonia are of great concern to the
eulogies or contributing to the eulogies of oth- surviving parent. They were helped as single
ers.41 They want to be active participants. parents to set limits, support, and encourage
These children often thought of the parent these children, sidestepping the provocative
208 CA A Cancer Journal for Clinicians
- 14. CA Cancer J Clin 2006;56:197–212
nature of the angry meltdowns. However, (2) View communication as a process, not a
home and parent remained important to the 9- one-time event. Communicating with children
to 11-year-old children. They needed to invest or adolescents about a parent’s terminal condi-
in activities outside the home while still retain- tion is best done through careful dosing of
ing a close bond. They still valued their parent’s information over time, which builds a pathway
love and support. A different dimension of of open communication and trust that children
stress and parental trial came from the adoles- will be informed in a timely way about major
cents who developmentally needed to separate changes in the parent’s functioning or progno-
sis. The level of detail communicated about the
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from parent and home.
The 9- to 11-year-olds, 12- to 14-year-olds, situation is greater with older than younger
and 15- to 17-year-olds spent much more time children. Physicians should encourage parents
away from home than younger children. The to provide open and hopeful, but not unreal-
istic information. Efforts to treat and care for
difference, however, is that the 9- to 11-year
the ill parent are emphasized, but the child
olds often moved to activities outside the
must also be assured of their own continued
home, while the 2 adolescent groups moved
care and love. The resulting dialogue helps
away from the close parental contact they pre-
children cope with the painful uncertainties
viously needed and enjoyed. that both parents and children must endure in
this highly stressful period.
RECOMMENDATIONS FOR HELPING CHILDREN
(3) Children and adolescents generally expe-
DURING A PARENT’S ILLNESS ACROSS rience emotional reactions intermittently and
DEVELOPMENTAL LEVELS for brief periods of time interspersed with rapid
return to normative functioning. Their capac-
Some general approaches to helping chil- ity for sustained or intense emotion is limited.
dren of all ages during a parent’s terminal illness Sustained, intense grief may reflect symptom-
include the following: atic responses to stress rather than health. Their
(1) Plan parent visits during a long hospital- intermittent grief, as well as positive memories
ization. While some retrospective studies have about the parent, have been found to continue
reported lingering distress in children from un- to emerge over the course of their develop-
planned visits with the hospitalized par- ment in response to additional stresses or de-
ent,24,25,29 others have found that planned velopmental advances.1,43,44
visits are often reassuring. In the MSKCC These and the more specific recommenda-
study, at 1-year follow up after the parent’s tions in Tables 2 and 3 are directed to physi-
cians and other health care professionals
death, most children who had participated in
treating life-threatening illnesses in patients
the intervention did not report lingering dis-
with children; pediatricians and psychiatrists
tress about planned visits.1 Others have de-
who may treat children with physical or psy-
scribed the importance of planning with the
chological symptoms of distress; and physicians
parent and the patient, if possible, for how the in palliative care programs and in hospices.
visit will go, limiting the time of the visit Many physicians will not have direct contact
depending on the developmental level of the with family members other than their adult
child and the physical and mental state of the patients and their spouses. However, integrated
parent, and informing the child about the treat- into competent end-of-life care is the aware-
ment and equipment they are seeing.42 While ness that the patient is distressed when the
children should be encouraged to visit the par- family is adversely impacted and that the pa-
ent at intervals that are not too disruptive to tient wants the health care team to assist with
their lives, pushing them to visit if they are their family’s needs. Finally the physician’s sup-
strongly opposed is generally not recom- port and appropriate use of direct services to
mended, unless it is the only opportunity for a families provided by other members of the
final visit. medical team promote effective family-
Volume 56 Y Number 4 Y July/August 2006 209
- 15. Helping Children Cope with a Parent’s Terminal Illness
TABLE 2 Recommended Guidelines for Families during a Parent’s Terminal Illness
3- to 5-year-olds
1. Gradually/consistently explain changes due to cancer and treatment without being overly optimistic/pessimistic. Children can learn “script” of events without fully
comprehending meaning and importance; at this age, death is not understood as permanent.
2. Separation from primary caregiver is major concern at this age.
3. Establish consistent time when child can ask questions and share feelings, such as bedtime.
4. Provide consistent substitute caregiving when primary caregiver is unavailable.
5. Use play and art to illustrate and concretize complex events that are occurring in family.
6. Having “a good cry together” may be frightening rather than cathartic for young children.
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7. Anticipate child’s increased separation anxiety and need for reassurance that they will be cared for.
8. Normalize intermittent, brief intense emotional expression—changing subject and going off to play are important safety valves.
9. Encourage planned, time-limited visits during prolonged parental hospitalizations. Assure child has toys, activities to do with ill parent and that parent’s condition,
limited capacity is explained.
10. Offer families consultation with social worker or other psychosocial professional for additional concerns.
6- to 8-year-olds
1. Provide timely information to children about parent’s illness; explain what child is seeing/hearing [eg, explain patient’s withdrawal is caused by illness, not lack of
love]. Once children believe their own view of events, it can be difficult to alter. Repetition is required.
2. Children can be overcome by parent’s strong anger or sadness. Controlled emotions are effective for discussing events.
3. Normalize high emotionality at this age.
4. Normalize children’s temporary reductions in school performance when stressed.
5. Engage other family, friends, social workers, or other psychosocial professionals able to listen to emotional concerns if parent has difficulty listening empathically
due to own distress.
6. Reassure child of parent’s strength and ability to provide care even when they express strong emotion.
7. Acknowledge situation’s uncertainty and difficulty for everyone. Anticipatory anxiety can occur at this age, and children need support that family will continue.
8. Reassure children that this is not their fault. Children blame themselves when bad things happen.
9. Communicate with the child’s teachers and other significant adults about parent’s illness.
10. Arrange consistent substitute caregiving with people who communicate well with child.
11. Prepare child for medical emergencies that may require parents to leave the house unexpectedly.
12. Children require permission to ask questions and express emotions they fear may upset others.
13. Normalize children’s need to maintain developmentally appropriate activities.
14. Remind parents of their central role in maintaining self-esteem by providing praise.
15. Prepare children to visit with parent in the hospital, explain what they are seeing, and make time for clarification afterward.
16. Consider professional consultation for children this age if severe anxiety, fear, school phobia, preoccupation with self-blame, or persistent depression and low self-
esteem occur.
9- to 11-year-olds
1. Give children fairly detailed information when parent’s diagnosis is verified: name of the disease, specifics, symptoms, known causes, treatments, possible side
effects—optimistic, hopeful communication, not unrealistic. Account for child’s observations.
2. Assure children the illness is not their fault.
3. Acknowledge the stress of uncertainty for everyone, as well as the strength of family unit.
4. Children this age may have feelings of sadness and loss about possibility of parent’s death.
5. Have child visit during prolonged hospitalizations. Suggest possible discussions; explain parent’s condition and treatment. Children this age can benefit from meeting
medical and nursing staff and from exploring the hospital environment.
6. Help child remain involved in after-school activities, sports, and ongoing contact with friends.
7. Support children’s interest in helping with patient’s care, but child should not be independently in charge of the parent’s care.
8. Remind parents that coalitions and special preferences within the family may cause distress.
9. Encourage children’s interest in reading or writing about the disease or treatment and their responses if they want to do this.
centered care. Families have been found to consequences and the enhancement of growth-
benefit from consultation with a social worker promoting components after the tragic loss of a
or psychosocial professional during periods of young parent.
high stress and expected loss.45,46 Three research directions for the 21st cen-
tury show promise for more specific and less
Future Directions confusing and contradictory findings:
(1) Studying developmentally homogeneous
The last decades of the 20th century con- subgroups of children and the differing effects
tributed greatly to knowledge about childhood of different types of deaths;
bereavement, but much remains to be under- (2) Conducting longer-term prospective
stood about the prevention of later adverse studies that include critical experiences (eg,
210 CA A Cancer Journal for Clinicians
- 16. CA Cancer J Clin 2006;56:197–212
TABLE 3 Recommended Guidelines for Families Following a Parent’s Death
3- to 5-year-olds
1. Use concrete details to describe the fact that when a person dies, all bodily functions cease and person does not come back.
2. Use play, drawing, and other expressive activities to enhance the child’s understanding.
3. Normalize emotions children and others might feel so they can respond in ways others will understand.
4. Describe what child can expect to happen, what role child can play, roles other people will play, how others will feel and behave, and how child may feel during
funerals and memorials. Encourage participation in these rituals.
5. Assign caretaker able to take child out after a brief time if indicated. Such ceremonies are often too long for most preschoolers.
6. Reinforce child’s need to continue positive activities.
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7. Reassure child about their ability and determination to provide continued love and care.
8. Provide transitional objects that seem important to child: deceased’s possessions, clothing, letters, or gifts they may have left for child.
9. Prepare for surge of separation anxiety, sleeping problems, desire to sleep with the surviving parent, clinging behavior, and other temporary regressive behaviors.
10. During first few weeks/months after the death, child may talk frequently about positive memories of parent and ask repeatedly where he/she has gone.
11. Use available groups or bereavement programs for child. Engage others to listen and respond to questions if the parent is overwhelmed with own grief.
6- to 8-year-olds
1. Inform even young children about parent’s worsening condition when death is imminent.
2. Consider final visit with patient—children value final expressions of love. Prepare by describing patient’s condition and suggesting what children can say or do. Just
touching the patient can be reassuring and helpful and exchanging gifts meaningful.
3. Provide empathic support for initial responses to parent’s death. Permit return to normative activities.
4. Have children attend traditional rituals and participate whenever possible.
5. Children this age may ask blunt questions around time of the death: “Are you a widow now?”
6. Children’s expressions of grief are often brief and episodic.
7. At this age, increased separation anxiety and sleeping difficulties are likely, often expressed also in stubbornness and problems with behavior.
8. Reassure children of parent’s strength and commitment to continued care and love of the children despite grief of surviving parent. Remember to praise child for their
efforts during such a difficult time.
9. Give children objects or possessions of parent who died to provide a sense of connection and solace.
10. Suggest participation in available bereavement programs.
11. Encourage discussion with other adults or professionals when parent is too distressed to listen to child’s often joyous remembrance.
12. Inform the school of the death and explore supportive services available to child should they become upset there.
9- to 11-year-olds
1. Normalize both emotional avoidance at this age and emotional outbursts sometimes followed by embarrassment.
2. Normalize increases in separation anxiety, behavioral and physical symptoms.
3. Invite children to participate in ceremonies, either directly or indirectly through writing about parent or describing their views to other presenters at the rituals. Parents
should be open to having their friends attend, as well.
4. Follow child’s lead about returning to school after the death; keep in mind, however, that staying out of school beyond the final ceremonies is usually not helpful.
5. Help child choose appropriate mementos belonging to the patient.
6. Reestablish family routines.
7. Teach and encourage mourning and participation in bereavement programs if available.
8. Inform school of death and explore supportive services available to their child there.
terminal stage in predictable deaths, later re- clarify when groups may be unknowingly
sponses) that may clarify different outcomes; combined whose findings cancel out clinically
and important variables.
(3) Combining qualitative and quantitative This century has great promise to provide a
analytic approaches provides a way to under- rich harvest of useful approaches to the psycho-
stand the realistic complexity of the area and logical support of children exposed to man-
populations under study. This may help to made and natural disasters, as well as diseases.
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